Progress of Ferrocene-Based Metal Cation Recognition Receptor

doi:10.6023/cjoc202005042

Abstract

Due to the rapid development of industry, the concentration of metal ions in water has increased significantly, thus causing a series of harm. Therefore, the research on ion recognition receptors and electrochemical sensors is favored by researchers. Ferrocene based metal compounds are considered to be very important metal cation recognition receptors due to their stability, favourable electrochemical property, reaction activity, and the synthesis method of ferrocene derivatives is very mature. From the aspects of raw materials, synthesis methods, molecular structure, etc., the research progress of ferro-cene-based cation recognition receptors in recent years is reviewed. It is mainly classified from different molecular recognition centers such as crown ethers, polyamines, conjugates and heterocycles. At last, the future and development of ferrocene receptors are prospected.

Key words: Keywords ferrocene, cation recognition, receptor, research progress

Cite this article

Yuting Liu, Jie Li, Dawei Yin. Progress of Ferrocene-Based Metal Cation Recognition Receptor[J]. Chinese Journal of Organic Chemistry, 2021, 41(1): 158-170.

Export EndNote|Reference Manager|ProCite|BibTeX|RefWorks

share this article

Fig. & Tab. 35

Scheme 1. Synthesis of ferrocenyl receptors 2 and 3

Scheme 2. Synthesis of ferrocenyl receptors 7 and 8 Reagents and conditions: (a) Cs2CO3, CH3CN, reflux; (b) active-C, FeCl3•6H2O, NH2NH2•H2O, ethanol, reflux; (c) chlorocarbonylferrocene, CH2Cl2, r.t.

Scheme 3. Synthesis of ferrocenyl receptor 9

Scheme 4. Synthesis of ferrocenyl receptor 10

Scheme 5. Synthesis of ferrocenyl receptor 12

Scheme 6. Synthesis of ferrocenyl receptor 16

Scheme 7. Synthesis of ferrocenyl receptors 18 and 19

Scheme 8. Synthesis of ferrocenyl receptors 20 and 21

Scheme 9. Synthesis of ferrocenyl receptors 22 and 23

Scheme 10. Synthesis of ferrocenyl receptors 24 and 25

Scheme 11. Synthesis of ferrocenyl receptor 27

Scheme 12. Synthesis of ferrocenyl receptors 29~32

Scheme 13. Synthesis of ferrocenyl receptor 34

Scheme 14. Synthesis of ferrocenyl receptor 36

Scheme 15. Synthesis of ferrocenyl receptor 37

Scheme 16. Synthesis of ferrocenyl receptors 39 and 40

Scheme 17. Synthesis of ferrocenyl receptors 42~45

Scheme 18. Synthesis of ferrocenyl receptor 46

Scheme 19. Synthesis of ferrocenyl receptors 47 and 48

Scheme 20. Synthesis of ferrocenyl receptor 49

Scheme 21. Synthesis of ferrocenyl receptor 50

Scheme 22. Synthesis of ferrocenyl receptors 51 and 52

Scheme 23. Synthesis of ferrocenyl receptor 54

Scheme 24. Synthesis of ferrocenyl receptor 55

Scheme 25. Synthesis of ferrocenyl receptor 57

Scheme 26. Synthesis of ferrocenyl receptors 69 and 60

Scheme 27. Synthesis of ferrocenyl receptor 62

Scheme 28. Synthesis of ferrocenyl receptor 63

Scheme 29. Synthesis of ferrocenyl receptor 64

Scheme 30. Synthesis of ferrocenyl receptor 66

Scheme 31. Synthesis of ferrocenyl receptor 67

Scheme 32. Synthesis of ferrocenyl receptors 68, 69

Scheme 33. Synthesis of ferrocenyl receptors 70 and 71

Scheme 34. Synthesis of ferrocenyl receptor 72

Scheme 35. Synthesis of ferrocenyl receptor 73

References 108

	Kealy T.J.; Pauson P.L.J. Nature 1951, 168, 1039.
	Huang Y.-J.; Lin J.-S.; Zhang W.-K.; Zhang B.-G.; Sun Q.-Z. Inorg. Chem. Commun. 2019, 105, 129.
	Liu Y.-T.; Yang L.-S.; Yin D.-W.; Dang Y.; Yang L.; Zou Q.; Li J.; Sun J.-X. J. Organomet. Chem. 2019, 899, 120903.
	Rajalakshmi A.V.; Palanisaml N. Spectrochim. Acta Part A, 2020, 228, 117812.
	Dewangan S.; Barik T.; Parida R.; Mawatwal S.; Dhiman R.; Giri S.; Chatterjee S. J. Organomet. Chem. 2019, 904, 120999.
	Wu K.-L.; Zhang W.-B.; Zhou D.; Xu Y. Chin. J. Org. Chem. 2014, 34, 1201.
	( 吴孔丽, 张吾斌, 周丹, 徐琰, 有机化学, 2014, 34, 1201.).
	Wang X.-X.; Qi Y.-X.; Shen Y.; Yuan Y.; Zhang L.; Zhang C.-Y.; Sun Y.-H. Sens. Actuators B, 2020, 310, 127756.
	Yu L.-J.; Wu L.; Wang L.-J.; Ren G.-L.; Nui L.; Guo H.-M. Chin. J. Anal. Lab. 2020, 39, 97.
	( 余利娇, 吴亮, 王丽娟, 任桂铃, 牛露, 郭浩模, 分析实验室, 2020, 39, 97.).
	Xiao W.-J.; Cao H.-Y.; Lin Y.; Liu W.-Q.; Wan P.-N.; Cui H.-F. Chin. J. Synth. Chem. 2020, (4),341.
	( 肖文杰, 曹海泳, 林艳, 刘文琴, 万屏南, 崔汉峰, 合成化学 2020 (4),341.)
	Kamal A.; Kumar K.; Kumar V.; Mahajan R.K. Electrochim. Acta. 2014, 145, 307.
	Qian C.; Chuo L.-P.; Zhao H.-Y.; Bian Z.-X. Chin. J. Org. Chem. 2017, 37, 2328.
	( 钱超, 绰洛鹏, 赵海英, 边占喜, 有机化学, 2017, 37, 2328.).
	Liu Y.-T.; Sheng J.; Yin D.-W.; Xin H.; Yang X.-M.; Qiao Q.-Y.; Yang Z.-J. J. Organomet. Chem. 2018, 856, 27.
	Jia D.-G.; Zheng J.-A.; Fan Y.-R.; Yu J.-Q.; Wu X.-L.; Wang B.-J.; Yang X.-B.; Huang Y. J. Organomet. Chem. 2019, 888, 16.
	Zhao H.-Y.; Yin F.-N.; Yu L.-Y.; Li B.-G.; Bian Z.-X. Chin. J. Org. Chem. 2016, 36, 1118.
	( 赵海英, 尹凤楠, 于玲岩, 李保国, 边占喜, 有机化学, 2016, 36, 1118.).
	Niu X.H.; Mo Z.L.; Yang X.; Shuai C.; Liu N.J.; Gou R.B. Bioelectrochemistry. 2019, 128, 74.
	Wang X.-C.; Xiao L.-F.; Wu J.-Y.; Li S.-L.; Tian Y.-P. J. Anhui Univ. (Nat. Sci). 20 17, 16, 28.
	( 汪徐春, 肖陆飞, 吴杰颖, 李胜利, 田玉鹏, 安徽大学学报(自然科学版), 2017, 16, 28.).
	Hong G.L.; Chen R.T.; Xu L.Y.; Xing L.; Yang Z.Q.; Zhou G.B.; Li L.; Chen W.; Peng H.P. Anal. Chim. Acta. 2020, 1099, 52.
	Minic A.; Bugarinovic J.P.; Pejovic A.; Komatina D.I.; Bogdanovic G.A.; Damljanovic I.; Stevanovic D. Tetrahedron Lett. 2018, 59, 3499.
[19]	Korotaev,V. Y.; Kutyashev, L. B.; Barkov, A. Y.; Rozhkova, Y. S.; Plekhanova, I. V.; Shklyaev, Y. V.; Sosnovskikh, V. Y. Tetrahedron Lett. 2019, 60, 150916.
[20]	Minic, A.; Walle, T. V.; Hecke, K. V.; Combrinck, J.; Smith, P. J.; Chibale, K.; D’hooghe, M. Eur. J. Med. Chem. 2020, 187, 111963.
[21]	Liu, Y.-T.; Xin, H.; Yin, J.-Y.; Yin, D.-W.; Yang, Z.-J.; Li, J. J. Mol. Struct. 2018, 1157, 482.
[22]	Tan, J.; Chen, L.; Peng, A.-L.; Xiao, J.; Zhang, E.-J. Chin. J. Mod. Appl. Pharm. 2018, 35, 345.
	谭娟, 陈灵, 彭安林, 肖静, 张恩景, 中国现代应用药学, 2018, 35, 345.
[23]	Ren, T.; Zhao, L.-J.; Zhong, R.-G. Chem. Reagents. 2020, 42, 797.
	任婷, 赵丽娇, 钟儒刚, 化学试剂, 2020, 42, 797.
[24]	Feng, L.-F.; Du, J.; Yao, C.-J.; Jiang, Z.-Q.; Li, T.; Zhang, Q.; Guo, X.-N.; Yu, M.; Xia, H.-L.; Shi, L.; Jia, J.-L.; Tong, Y.; Ju, L.; Liu, J.-Q.; Lou, J.-L.; Lemos, B. Environ. Int. 2020, 138, 105593.
[25]	Ni, P.-W. M. S. Thesis, Lanzhou Jiaotong Universiy, Lanzhou , 2019. (倪朋伟, 硕士论文, 兰州交通大学, 兰州, 2019. ).
[26]	Huang, Y.-J.; Lin, J.-S.; Zhang, W.-K.; Zhang, B.-G.; Sun, Q.-Z. Inorg. Chem. Commun. 2019, 105, 129.
[27]	Liu, T.; Liu, X.; Spring, D. R.; Qian, X.; Cui, J.; Xu, Z. Sci. Rep. 2014, 4, 5418.
[28]	Qu, F.-M.; Chen, F.; Hou, X.-Z.; Ma, X.-Y. Chin. J. Appl. Chem. 2013, 30, 1393. (in Chinese)
	屈枫锦, 陈芳, 候秀璋, 马晓燕, 应用化学, 2013, 30, 1393.
[29]	Wang, C.; Wu, J.; Jiang, K.; Humphrey, M. G.; Zhang, C. Sens. Actuator B, 2017, 238, 1136.
[30]	Saleem, M.; Yu, H.; Wang, L.; Zain-ul-Abdin.; Khalid, H.; Akram, M.; Abbasi, N. M.; Chen, Y. J. Electroanal. Chem. 2016, 763, 71.
[31]	Sokolov, V. I. Chin. J. Org. Chem. 2018, 38, 75. (in Chinese)
	Sokolov, V.I. 有机化学, 2018, 38, 75.
[32]	Shi, X.-R. Chin. J. Synth. Chem. 2017, 25, 985. (in Chinese)
	石翛然, 合成化学, 2017, 25, 985.
[33]	Liu, Y. F.; Hu, J. F.; Teng, Q.; Zhang, H. Sens. Actuators, B, 2017, 238, 166.
[34]	Dang, Y. M. S. Thesis, Shaanxi University of Science & Technology, Xi'an , 2020. (党阳, 硕士论文, 陕西科技大学, 西安, 2020). (in Chinese)
[35]	Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 2495.
[36]	Ahmed, A.; Hashmi, M. A.; Ayub, K. J. Mol. Liq. 2020, 302, 112577.
[37]	Korchowiec, B.; Trojan, S.; Joly, J.-P.; Korchowiec, J.; Beley, M.; Rogalska, E. Thin Solid Films 2019, 683, 49.
[38]	Oliveira, E. Santos, H. M. Dyes Pigm. 2016, 135, 3.
[39]	Li, J.; Yim, D.; Jang, W.-D.; Yoon, J.-Y. Chem. Soc. Rev. 2017, 46, 2437.
[40]	Tian, X.; Yang, F.-Q.; Yuan, W.; Zhao, L.; Yao, L.; Zhen, X.-L.; Han, J.-R.; Liu, S.-X. Chem. J. Chin. Univ. 2020, 41, 490. (in Chinese)
	田霞, 杨福群, 袁伟, 赵雷, 姚雷, 甄小丽, 韩建荣, 刘守信, 高学校化学学报 2020, 41, 490.
[41]	Agurto, N.; Maldonado, T.; Godoy, F.; Gomez, A.; Silva, C. P.; Pavez, J.; Ferraudi, G.; Oliver, A.; Lappin, A. G. J. Organomet. Chem. 2017, 827, 32.
[42]	Xiong, J.; Tan, M.-K.; Lu, S.-F.; Li, M.; Yang, S.-B. Chin. J. Inorg. Chem. 2019, 35, 1805. (in Chinese)
	熊俊, 谭茂坤, 吕少仿, 李明, 杨水彬, 无机化学学报, 2019, 35, 1805.
[43]	Pizarro, J.; Flores, E.; Jimenez, V.; Maldonado, T.; Saitz, C.; Vega, A.; Godoy, F.; Segura, R. Sens. Actuators, B, 2019, 281, 115.
[44]	Xu, W.-N. M. S. Thesis, Shandong Normal Universiy, Jinan , 2008.(徐伟娜, 硕士论文, 山东师范大学, 济南, 2008). (in Chinese)
[45]	Hu, L. M. S. Thesis, Shandong Normal Universiy, Jinan , 2019. (胡玲, 硕士论文, 山东师范大学, 济南, 2019). (in Chinese)
[46]	Hong, B.-J. M. S. Thesis, Fujian Normal Universiy, Fuzhou , 2010. (洪碧琼, 硕士论文, 福建师范大学, 福州, 2010. ). (in Chinese)
[47]	Zhang, L.-J. M. S. Thesis, Shandong Normal Universiy, Jinan , 2012. (in Chinese) (张丽静, 硕士论文, 山东师范大学, 济南, 2012).
[48]	Dagdevren, M.; Yilmaz, I.; Yucel, B.; Emirik, M. J. Phys. Chem. B. B, 119, 12464.
[49]	Alcay, Y.; Yavuz, O.; Gelir, A.; Atasen, S. K.; Karaoglu, K.; Yucel, B.; Tuzun, N. S.; Yilmaz, I. J. Organomet. Chem. 2018, 868, 131.
[50]	Flores, E.; Pizarro, J.; Godoy, F.; Segura, R.; Gomez, A.; Agurto, N.; Sepulveda, P. Sens. Actuators, 2017, 251, 433.
[51]	Agurto, N.; Silva, C. P.; Jara, G. S.; Maldonado, T.; Flores, E.; Morales, C. F.; Oliver, A.; Godoy, F.; Pavez, J. Electrochim Acta. 2019, 318, 479.
[52]	Ferreira, J. F.; Bagatin, I. A. Spectrochim. Acta, Part A, 2018, 189, 44.
[53]	Toyama, M.; Fujii, Y.; Endo, M. Inorg. Chim. Acta 2019, 486, 304.
[54]	Lukasik, N.; Chojnacki, J.; Luboch, E.; Okuiewski, A.; Wagner-Wysiecka, E. J. Photochem. Photobiol., A., 2020, 390, 112307.
[55]	Wang, X.-B.; Xiong, H.-J.; Wu, S.-S.; Geng, Z.-R.; Wang, Z.-L. Chin. J. Inorg. Chem. 2020, 36, 1035. (in Chinese)
	王小波, 熊慧娟, 吴莎莎, 耿志荣, 王志林, 无机化学学报, 2020, 36, 1035.
[56]	Parthiban, C.; Elango, K. P. Spectrochim. Acta., Part A, 2017, 174, 147.
[57]	Moshikur, R. M.; Chowdhury, M. R. Wakabayashi, R.; Tahara, Y.; Kamiya, N.; Moniruzzaman, M.; Goto, M. J. Mol. Liq. 2020, 299, 112166.
[58]	Wu, F.-H.; Yang, J.-Q.; Xu, F.; Dong, T.-Y.; Chen, C.; Chu, X.-P. Anal. Sci. 2019, 35, 239. (in Chinese).
	吴芳辉, 杨俊卿, 徐帆, 董天涯, 陈晨, 储心萍, 分析科学学报, 2019, 35, 239.
[59]	Huang, Y.-J.; Lin, J.-S.; Zhang, W.-K.; Zhang, B.-G.; Sun, Q.-Z. Inorg. Chem. Commun. 2019, 105, 129.
[60]	Dewangan, S.; Barik, T.; Parida, R.; Mawatwal, S.; Dhiman, R.; Giri, S.; Chatterjee, S. J. Organomet. Chem. 2019, 904, 120999.
[61]	Feng, W.-H.; Qiao, C.-J.; Ran, C.-L.; Du, W.; Xu, Y.; Fan, Y.-T. Chin. J. Synth. Chem. 2010, 18, 429. (in Chinese)
	冯文浩, 乔纯杰, 冉春玲, 杜薇, 徐琰, 樊耀亭, 合成化学, 2010, 18, 429.
[62]	Devaraj, S.; Elanchezhian, V. S.; Kandaswamy, M. Inorg. Chem. Commun. 2011, 14, 1596.
[63]	Uahengo, V.; Xiong, B.; Zhao, P.-P.; Zhang, Y.; Cai, P.; Hu, K.; Cheng, G.-Z. Sens. Actuators, B 2014, 190, 937.
[64]	Huang, M.; Lou, Z.-W.; Peng, X.-Q.; He, H.-P.; Zhang, X.-H.; Wang, S.-F. Chin. J. Org. Chem. 2015, 35, 1966. (in Chinese)
	黄敏, 娄兆文, 彭小倩, 何汉平, 张修华, 王升富, 有机化学, 2015, 35, 1966.
[65]	Qi, S. M. S. Thesis, Shanghai Institute of Technology, Shanghai , 2016.(亓帅, 硕士论文, 上海应用技术大学, 上海, 2016). (in Chinese)
[66]	Li, P.-Q. M. S. Thesis, Hebei University of Science and Technology, Shijiazhuang , 2018. (李鹏起, 硕士论文, 河北科技大学, 石家庄, 2018). (in Chinese)
[67]	Dong, J.-Y. M. S. Thesis, Inner Mongolia University, Hohhot , 2019. (in Chinese)(董均阳, 硕士论文, 内蒙古大学, 呼和浩特, 2019).
[68]	Bao, X.-F.; Cao, X.-W.; Nie, X.-M.; Xu, Y.; Cuo, W.-H.; Zhou, B.-J.; Zhang, L.; Liao, H.; Pang, T. Sens. Actuators, B,2015, 208, 54.
[69]	Mathivanan, M.; Tharmalingam, B.; Mani, K. S.; Thiagarajan, V.; Murugesapandian, B. Spectrochim. Acta, Part A, 2020, 234, 118235.
[70]	Guo, X.-L.; Li, J.; Li, X.; Guo, L.-L.; Zhao, L.-P.; Hou, X.-F. Chem. Reagents 2020, 42, 976. (in Chinese).
	郭心灵, 李静, 李玄, 郭磊磊, 赵丽平, 侯旭峰, 化学试剂, 2020, 42, 976.
[71]	Tong, L.; Sun, S.-H.; Qiao, M.; Fan, J.; Ding, L.-P. J. Photochem. Photobiol., A., 2019, 374, 131.
[72]	Li, C.-T.; Wang, M.-M.; Zhu, Q.; Cao, Q.-Y. Chin. J. Org. Chem. 2017, 37, 1443. (in Chinese).
	李春涛, 王蒙蒙, 朱倩, 曹迁永, 有机化学, 2017, 37, 1443.
[73]	Zhao, X.-F.; Cao, Q.-Y.; Lu, X.; Yang, Z.-Y.; Tang, J.-C. Acta Chim Sinica. 2012, 70, 838. (in Chinese).
	赵小芳, 曹迁永, 卢鑫, 杨震宇, 唐建成, 化学学报, 2012, 70, 838.
[74]	Wang, J.-C.; Wu, X.-F.; Jiao, X.-L.; Wang, M. Chin. J. Synth. Chem. 2014, 22, 174. (in Chinese).
	王健春, 邬孝芳, 焦晓兰, 王梦, 合成化学, 2014, 22, 174.
[75]	Arivazhagan, C.; Borthakur, R.; Ghosh. S. Organometallics 2015, 34, 1147.
[76]	Fang, Y.; Zhou, Y.; Rui, Q.-Q.; Yao, C. Organometallics 2015, 34, 2962.
[77]	Teng, Q.; Liu, Y.-F.; Hu, J.-F.; Chai, H.; Li, K.-F.; Zhang, H. J. Tetrahedron 2016, 72, 3890.
[78]	Liu, Y.-F.; Teng, Q.; Hu, J.-F.; Sun, R.-F.; Zhang, H. Sens. Actuator, B,2016, 234, 680.
[79]	Liu, Y.-F.; Hu, J.-F.; Teng, Q.; Zhang, H. Sens. Actuators B, 2017, 238, 166.
[80]	Zhou, Y.-Y.; Cao, Y.; Cong, G.-D.; Zhang, Y.-J.; Zhao, H.-H.; Gao, X.-X.; Zhao, G. Inorg. Chem. Commun. 2018, 96, 170.
[81]	Ling, L. Ph. D. Dissertation, Inner Mongolia University, Hohhot , 2019. (in Chinese)(伶俐, 博士论文, 内蒙古大学, 呼和浩特, 2019).
[82]	Zi, J.-X. M. S. Thesis, Inner Mongolia University, Hohhot , 2019. (in Chinese) (訾婧欣, 硕士论文, 内蒙古大学, 呼和浩特, 2019).
[83]	Kim, M.; Mergu, N.; Son, Y.-A. J. Lumin. 2018, 204, 244.
[84]	Wang, N.; Arulkumar, M.; Chen, X.-Y.; Wang, B.-W.; Chen, S.-H.; Yao, C.; Wang, Z.-Y. Chin. J. Org. Chem. 2019, 39, 2771. (in Chinese).
	王能, Arulkumar, M, 陈孝云, 王柏文, 陈思鸿, 姚辰, 汪朝阳, 有机化学, 2019, 39, 2771.
[85]	Alfonso, M.; Tarraga, A.; Molina, P. Tetrahedron Lett. 2016, 57, 3053.
[86]	Cao, Z.-Y.; Fan, X.; Yang, Z.-Y.; Zhang, X.-B.; Ding, N.-X.-J.; Ding, Y.-B. Sens. Actuators, B 2020, 310, 127855.
[87]	Xiao, L.-W.; Ren, P.; Jing, X.-M.; Ren, L.-L.; Li, Z.; Dai, F.-C. Chin. J. Org. Chem. 2017, 37, 3085. (in Chinese).
	肖立伟, 任萍, 景学敏, 任丽磊, 李政, 戴富才, 有机化学, 2017, 37, 3085.
[88]	Rangasamy, M.; Palaninathan, K. Inorg. Chem. Commun. 2019, 101, 177.
[89]	Wang, M.-G.; Peng, J.-X.; Liu, C.-P.; Zheng, M.-Y.; Wang, Y.-X.; Duan, Z.-Y. Chem. Ind. Eng. Prog. 2019, 38, 1941. (in Chinese).
	王梅阁, 彭家祥, 刘成鹏, 郑美玉, 王雅萱, 化工进展 2019, 38, 1941.
[90]	Bhatta, S. R.; Pal, A.; Sarangi, U. K.; Thakur, A. Inorg. Chim. Acta. 2019, 498, 119097.
[91]	Shi, L.; Song, W.; Li, Y.; Li, D.-W.; Swanick, K. N.; Ding, Z.-F.; Long, Y.-T. J. Talanta 2011, 84, 900.
[92]	Alfonso, M.; Tarraga, A.; Molina, P. J. Org. Chem. 2011, 76, 939.
[93]	Alfonso, M.; Espinosa, A.; Tarraga, A.; Molina, P. Org. Lett. 2011, 13, 2078.
[94]	Alfonso, M.; Tarraga, A.; Molina, P. J. Inorg. Chem. 2013, 52, 7487.
[95]	Thakur, A.; Ghosh, S. Organometallics 2012, 31, 819.
[96]	Sathyaraj, G.; Muthamilselvan, D.; Kiruthika, M.; Weyhermuller, T.; Nair, B. U. J. Organomet. Chem. 2012, 716, 150.
[97]	Romero, T.; Orenes, R. A.; Tarraga, A.; Molina, P. Organometallics 2013, 32, 5740.
[98]	Kumar, C. K.; Trivedi, R.; Kumar, K. R.; Giribabu, L.; Sridhar, B. Eur. J. Inorg. Chem. 2013, 35, 6019.
[99]	Kumar, C. K.; Trivedi, R.; Giribabu, L.; Niceditha, S.; Bhanuprakash, K.; Sridhar, B. J. Organomet. Chem. 2015, 780, 20.
[100]	Thakur, A.; Mandal, D.; Ghosh, S. J. Anal. Chem. 2013, 85, 1665.
[101]	Wang, Z.-C.; Dai, B.-N.; Qiu, J.-F.; Cao, Q.-Y.; Ge, J.-Z. Chin. J. Org. Chem. 2015, 35, 2383. (in Chinese).
	王智成, 戴博娜, 丘继芳, 曹迁永, 葛金柱, 有机化学, 2015, 35, 2383.
[102]	Bhatta, S. R.; Bheemireddy, V.; Vijaykumar, G.; Debnath, S.; Thakur, A. Organometallics 2017, 36, 2141.
[103]	Wu, X.-F.; Wu, P.; Li, J.-Y.; Lu, Q.; Wang, J.-C. Chin. J. Org. Chem. 2017, 37, 1412. (in Chinese).
	邬孝芳, 武沛, 李敬瑜, 陆婧, 王健春, 有机化学, 2017, 37, 1412.
[104]	Ren, Y.-P.; Liu, X.; Wang, R.; Zhou, Y.-Q.; Li, B.; Xu, Y.; Song, M.-P. Chin. J. Org. Chem. 2017, 37, 110. (in Chinese).
	任亚平, 刘絮, 王瑞, 周元清, 李标, 徐琰, 宋毛平, 有机化学, 2017, 37, 110.
[105]	Hou, J.-N. M. S. Thesis, Inner Mongolia University of Technology, Hohhot , 2018. (候静娜, 硕士论文, 内蒙古工业大学, 呼和浩特, 2018). (in Chinese)
[106]	Sun, Q. M. S. Thesis, Inner Mongolia University, Hohhot , 2018. (孙琦, 硕士论文, 内蒙古大学, 呼和浩特, 2018).
[107]	Jia, H.-J.; Han, L.-M.; Zhu, N.; Gao, Y.-Y.; Wang, Y.-Q.; Suo, Q.-L. Chin. J. Org. Chem. 2019, 39, 1753. .
	贾慧劼, 韩利民, 竺宁, 高媛媛, 王亚琦, 索全伶, 有机化学, 2019, 39, 1753.
[108]	Xu, J.-W.; Yang, T.-Q.; Baigude, H.; Zhao, H.-Y. Spectrochim. Acta, Part A 2020, 229, 117880.

[1]	Jingyi Wang, Jinyu Liu, Dongsheng Chen, Huayan Chen, Xin Xie, Fajun Nan. Design, Synthesis, and Structure-Activity Relationship of Novel Potent and Highly Selective Cysteinyl Leukotriene Receptor 1 (CysLT₁R) Antagonists [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 259-276.
[2]	Xiaoying Jia, Jiaxia Pu, Lirong Han, Qinghan Li. Research Progress in the Synthesis of Benzo[d]pentamembered Heterocyclic Thioethers Containing Two Heteroatoms [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 18-40.
[3]	Jiaxia Pu, Xiaoying Jia, Lirong Han, Qinghan Li. Research Progress of Visible Light Promoted C—N Bond Fracture to Construct C—C Bond [J]. Chinese Journal of Organic Chemistry, 2023, 43(8): 2591-2613.
[4]	Zujia Lu, Jian Qin, Jinting Wu, Wenli Cao, Baolong Kuang, Jianguo Zhang. Advances in the Synthesis of Energetic Compounds Based on 1,2,3-Triazoles [J]. Chinese Journal of Organic Chemistry, 2023, 43(2): 526-554.
[5]	Peng Liu, Fuming Zhong, Lihao Liao, Weiqiang Tan, Xiaodan Zhao. Progress in the Construction of Spirocyclohexadienones via Alkyne-Involving Dearomatization [J]. Chinese Journal of Organic Chemistry, 2023, 43(12): 4019-4035.
[6]	Donghang Shen, Xin Li, Shimeng Guo, Xin Xie, Fajun Nan. Design and Synthesis Studies of α-Methylene-γ-butyrolactones Antagonists of GPR52 [J]. Chinese Journal of Organic Chemistry, 2023, 43(11): 3916-3929.
[7]	Tianpeng Ge, Yanchen Yang, Chunpu Li, Jian Zhang, Hong Liu. Research Progress of Discoid Domain Receptor 1 (DDR1) Inhibitors [J]. Chinese Journal of Organic Chemistry, 2022, 42(9): 2760-2773.
[8]	Guangping Liang, Wei Wang, Xuxiu Zhu, Guangyan Liang, Jun Yang, Daoping Wang. Synthesis and in Vitro Anti-tumor Activity of Novel Spliced Compounds of Zidovudine and 4-Anilinoquinazolines [J]. Chinese Journal of Organic Chemistry, 2022, 42(9): 2793-2805.
[9]	Junzhe Yang, Zichao Xu, Chunpu Li, Yuanzheng Cheng, Hong Liu. Research Progress of Tropomyosin Receptor Kinase (TRK) Inhibitors [J]. Chinese Journal of Organic Chemistry, 2022, 42(7): 2055-2069.
[10]	Can Yong, Yun Li, Tao Bi, Guofeng Chen, Dongxia Zheng, Zhouyu Wang, Yuanyuan Zhang. Research Progress on the Synthesis and Activity of D-Galactose Derived Small Galectin Inhibitors [J]. Chinese Journal of Organic Chemistry, 2022, 42(5): 1307-1325.
[11]	Zhihao Zhang, Xin Jiang, Qinghan Li. Recent Progress in the Synthesis of Substituted Benzo[b]furan Derivatives [J]. Chinese Journal of Organic Chemistry, 2022, 42(4): 945-964.
[12]	Sha Zhou, Mukuo Wang, Weibin Xie, Shaa Zhou, Lixia Xiong, Yu Zhao, Zhengming Li. Synthesis and Insecticidal Activities of Novel Optically Active Dicarboxamides Containing N-Trifluoroacetyl Sulfulimiyl Substituents [J]. Chinese Journal of Organic Chemistry, 2021, 41(9): 3532-3538.
[13]	Changxing Ji, Guangxia Wang, Hua Wang. Progress in Metal-Organic Supramolecular System Based on Subcomponent Self-Assembly [J]. Chinese Journal of Organic Chemistry, 2021, 41(6): 2261-2279.
[14]	Wang Shoufeng, Wang Wengui. Recent Advances of the Construction of Trifluoromethylated Quaternary Carbon Center [J]. Chinese Journal of Organic Chemistry, 2020, 40(7): 1901-1911.
[15]	Jia Qianfa, Li Yaqiong, Lin Yinhe. Recent Advances in Organocatalyzed Aromatization Reactions [J]. Chinese Journal of Organic Chemistry, 2020, 40(6): 1502-1513.

基于二茂铁的金属阳离子识别受体的研究进展